ENST00000264381.8:c.1584T=
MANE Select
|
ENSP00000264381.3:p.Tyr528=
|
|
ENST00000264381.7:c.1584T=
|
ENSP00000264381.3:p.Tyr528=
|
|
ENST00000479451.5:c.174T=
|
ENSP00000418325.1:p.Tyr58=
|
|
ENST00000482958.1:c.*90T=
|
ENSP00000419804.1:n.*90T=
|
|
ENST00000488954.1:c.174T=
|
ENSP00000418504.1:p.Tyr58=
|
|
ENST00000497011.5:c.1584T=
|
ENSP00000419505.1:p.Tyr528=
|
|
NM_000055.2:c.1584T=
|
NP_000046.1:p.Tyr528=
|
|
XM_005247685.1:c.1707T=
|
XP_005247742.1:p.Tyr569=
|
|
NM_000055.3:c.1584T=
|
NP_000046.1:p.Tyr528=
|
|
NR_137635.1:n.226T=
|
|
|
NR_137636.1:n.1751T=
|
|
|
NM_000055.4:c.1584T=
MANE Select
|
NP_000046.1:p.Tyr528=
|
|
NR_137635.2:n.177T=
|
|
|
NR_137636.2:n.1702T=
|
|
|